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HRP20211225T1 - SULPHONILUREAS AND RELATED COMPOUNDS AND THEIR USE - Google Patents

SULPHONILUREAS AND RELATED COMPOUNDS AND THEIR USE Download PDF

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Publication number
HRP20211225T1
HRP20211225T1 HRP20211225TT HRP20211225T HRP20211225T1 HR P20211225 T1 HRP20211225 T1 HR P20211225T1 HR P20211225T T HRP20211225T T HR P20211225TT HR P20211225 T HRP20211225 T HR P20211225T HR P20211225 T1 HRP20211225 T1 HR P20211225T1
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Croatia
Prior art keywords
disease
alkyl
independently selected
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compound according
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HRP20211225TT
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Croatian (hr)
Inventor
Luke O'neill
Matthew Cooper
Avril Robertson
Kate SCHRODER
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The University Of Queensland
The Provost, Fellows, Foundation Scholars, and the other members of Board, of the College of the Holy& Undiv. Trinity of Queen Elizabeth near Dublin
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Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=56691944&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HRP20211225(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority claimed from AU2015900507A external-priority patent/AU2015900507A0/en
Application filed by The University Of Queensland, The Provost, Fellows, Foundation Scholars, and the other members of Board, of the College of the Holy& Undiv. Trinity of Queen Elizabeth near Dublin filed Critical The University Of Queensland
Publication of HRP20211225T1 publication Critical patent/HRP20211225T1/en

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    • C07D309/08Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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Claims (20)

1. Spoj formule (I), ili njegova farmaceutski prihvatljiva sol ili solvat: [image] pri čemu je W odabran od O, S i Se; J je odabran od S i Se; R1 je odabran iz skupine koja se sastoji od 5-eročlanog i 6-eročlanog heterociklila, koji svi mogu biti po izboru supstituirani, pri čemu je bilo koji izborni supstituent neovisno odabran iz skupine koju čine C1-10 alkil; C3-6 cikloalkil; hidroksialkil; C1-10 alkoksi; C2-10 alkenil; C2-10 alkinil; C6-C12 aril; ariloksi; heteroaril; heterociklil; halo; hidroksil; halogenirani alkil; amino; alkilamino; arilamino; acil; amido; CN; NO2; N3; CH20H; CONH2; CONR24R25; CO2R24; CH2OR24; NHCOR24; NHCO2R24; C1-3 alkiltio; sulfat; sulfonska kiselina; sulfonatni esteri; fosfonska kiselina; fosfat; fosfonat; mono-, di- ili trifosfatni esteri; tritil; monometoksitrtil; R24SO; R24S02; CF3S; CF3SO2; i trialkilsilil; pri čemu su R24 i R25 svaki neovisno odabrani između H i C1-10 alkila; R2 je odabran između 2,6-dialkilfenil, 2,6-dialkil-4-halofenil, 2,6-dicikloalkilfenil, 2,6-dicikloalkil-4-halofenil i: [image] pri čemu se svaka incidencija Y neovisno bira između C, N, S i O, koji se prema potrebi mogu supstituirati, pri čemu se bilo koji izborni supstituent neovisno bira iz skupine koja se sastoji od C1-10 alkil; C3-6 cikloalkil; hidroksialkil; C1-10 alkoksi; C2-10 alkenil; C2-10 alkinil; C6-C12 aril; ariloksi; heteroaril; heterociklil; halo; hidroksil; halogenirani alkil; amino; alkilamino; arilamino; acil; amido; CN; NO2; N3; CH20H; CONH2; CONR24R25; CO2R24; CH2OR24; NHCOR24; NHCO2R24; C1-3 alkiltio; sulfat; sulfonska kiselina; sulfonatni esteri; fosfonska kiselina; fosfat; fosfonat; mono-, di- ili trifosfatni esteri; tritil; monometoksitrtil; R24SO; R24S02; CF3S; CF3SO2; i trialkilsilil; pri čemu su R24 i R25 svaki neovisno odabrani između H i C1-10 alkila; R5 je odabran iz skupine koju čine vodik, halo, cijano, amid, sulfonamid, acil, hidroksil, C1-C6 alkil, C1-C6 haloalkil, C3-C5 ciloalkil i C1-C6 alkoksi, koje sve skupine mogu biti po želji supstituirane, prema potrebi, s halo, cijano ili C1-C6 alkoksi; i oba R1 su izravno vezana za J, a R2 je izravno vezan za susjedni dušik, preko atoma ugljika.1. Compound of formula (I), or its pharmaceutically acceptable salt or solvate: [image] wherein W is selected from O, S and Se; J is selected from S and Se; R 1 is selected from the group consisting of 5-membered and 6-membered heterocyclyl, all of which may be optionally substituted, wherein any optional substituent is independently selected from the group consisting of C 1-10 alkyl; C3-6 cycloalkyl; hydroxyalkyl; C1-10 Alkoxy; C2-10 alkenyl; C2-10 alkynyl; C6-C12 aryl; aryloxy; heteroaryl; heterocyclyl; halo; hydroxyl; halogenated alkyl; amino; alkylamino; arylamino; acyl; amido; CN; NO2; N3; CH2OH; CONH2; CONR24R25; CO2R24; CH2OR24; NHCOR24; NHCO2R24; C1-3 alkylthio; sulfate; sulfonic acid; sulfonate esters; phosphonic acid; phosphate; phosphonate; mono-, di- or triphosphate esters; trityl; monomethoxytrtyl; R24SO; R24S02; CF3S; CF3SO2; and trialkylsilyl; wherein R 24 and R 25 are each independently selected from H and C 1-10 alkyl; R 2 is selected from 2,6-dialkylphenyl, 2,6-dialkyl-4-halophenyl, 2,6-dicycloalkylphenyl, 2,6-dicycloalkyl-4-halophenyl and: [image] wherein each incidence of Y is independently selected from C, N, S, and O, which may optionally be substituted, wherein any optional substituent is independently selected from the group consisting of C1-10 alkyl; C3-6 cycloalkyl; hydroxyalkyl; C1-10 Alkoxy; C2-10 alkenyl; C2-10 alkynyl; C6-C12 aryl; aryloxy; heteroaryl; heterocyclyl; halo; hydroxyl; halogenated alkyl; amino; alkylamino; arylamino; acyl; amido; CN; NO2; N3; CH2OH; CONH2; CONR24R25; CO2R24; CH2OR24; NHCOR24; NHCO2R24; C1-3 alkylthio; sulfate; sulfonic acid; sulfonate esters; phosphonic acid; phosphate; phosphonate; mono-, di- or triphosphate esters; trityl; monomethoxytrtyl; R24SO; R24S02; CF3S; CF3SO2; and trialkylsilyl; wherein R 24 and R 25 are each independently selected from H and C 1-10 alkyl; R5 is selected from the group consisting of hydrogen, halo, cyano, amide, sulfonamide, acyl, hydroxyl, C1-C6 alkyl, C1-C6 haloalkyl, C3-C5 cycloalkyl and C1-C6 alkoxy, all of which groups may be optionally substituted, optionally, with halo, cyano or C1-C6 alkoxy; and both R1 are directly attached to J, and R2 is directly attached to the adjacent nitrogen, via a carbon atom. 2. Spoj u skladu s patentnim zahtjevom 1, naznačen time što R1 je 6-člani heterociklil, koji može biti prema potrebi supstituiran, pri čemu je bilo koji izborni supstituent neovisno odabran iz skupine koja se sastoji od C1-10 alkil; C3-6 cikloalkil; hidroksialkil; C1-10 alkoksi; C2-10 alkenil; C2-10 alkinil; C6-C12 aril; ariloksi; heteroaril; heterociklil; halo; hidroksil; halogenirani alkil; amino; alkilamino; arilamino; acil; amido; CN; NO2; N3; CH2OH; CONH2; CONR24R25; CO2R24; CH2OR24; NHCOR24; NHCO2R24; C1-3 alkiltio; sulfat; sulfonska kiselina; sulfonatni esteri; fosfonska kiselina; fosfat; fosfonat; mono-, di- ili trifosfatni esteri; tritil; monometoksitrtil; R24SO; R24SO2; CF3S; CF3SO2; i trialkilsilil; pri čemu su R24 i R25 svaki neovisno odabrani između H i C1-10 alkila.2. A compound according to claim 1, characterized in that R1 is a 6-membered heterocyclyl, which can be optionally substituted, wherein any optional substituent is independently selected from the group consisting of C1-10 alkyl; C3-6 cycloalkyl; hydroxyalkyl; C1-10 Alkoxy; C2-10 alkenyl; C2-10 alkynyl; C6-C12 aryl; aryloxy; heteroaryl; heterocyclyl; halo; hydroxyl; halogenated alkyl; amino; alkylamino; arylamino; acyl; amido; CN; NO2; N3; CH2OH; CONH2; CONR24R25; CO2R24; CH2OR24; NHCOR24; NHCO2R24; C1-3 alkylthio; sulfate; sulfonic acid; sulfonate esters; phosphonic acid; phosphate; phosphonate; mono-, di- or triphosphate esters; trityl; monomethoxytrtyl; R24SO; R24SO2; CF3S; CF3SO2; and trialkylsilyl; wherein R 24 and R 25 are each independently selected from H and C 1-10 alkyl. 3. Spoj prema bilo kojem od prethodnih zahtjeva, naznačen time, da je R1 potpuno zasićeni heterociklil, koji može biti prema potrebi supstituiran, pri čemu je bilo koji izborni supstituent neovisno odabran iz skupine koja se sastoji od C1-10 alkil; C3-6 cikloalkil; hidroksialkil; C1-10 alkoksi; C2-10 alkenil; C2-10 alkinil; C6-C12 aril; ariloksi; heteroaril; heterociklil; halo; hidroksil; halogenirani alkil; amino; alkilamino; arilamino; acil; amido; CN; NO2; N3; CH2OH; CONH2; CONR24R25; CO2R24; CH2OR24; NHCOR24; NHCO2R24; C1-3 alkiltio; sulfat; sulfonska kiselina; sulfonatni esteri; fosfonska kiselina; fosfat; fosfonat; mono-, di- ili trifosfatni esteri; tritil; monometoksitrtil; R24SO; R24SO2; CF3S; CF3SO2; i trialkilsilil; pri čemu su R24 i R25 svaki neovisno odabrani između H i C1-10 alkila.3. A compound according to any of the preceding claims, characterized in that R1 is fully saturated heterocyclyl, which may be optionally substituted, wherein any optional substituent is independently selected from the group consisting of C1-10 alkyl; C3-6 cycloalkyl; hydroxyalkyl; C1-10 Alkoxy; C2-10 alkenyl; C2-10 alkynyl; C6-C12 aryl; aryloxy; heteroaryl; heterocyclyl; halo; hydroxyl; halogenated alkyl; amino; alkylamino; arylamino; acyl; amido; CN; NO2; N3; CH2OH; CONH2; CONR24R25; CO2R24; CH2OR24; NHCOR24; NHCO2R24; C1-3 alkylthio; sulfate; sulfonic acid; sulfonate esters; phosphonic acid; phosphate; phosphonate; mono-, di- or triphosphate esters; trityl; monomethoxytrtyl; R24SO; R24SO2; CF3S; CF3SO2; and trialkylsilyl; wherein R 24 and R 25 are each independently selected from H and C 1-10 alkyl. 4. Spoj prema bilo kojem od prethodnih zahtjeva, naznačen time, da R1 je dušikov heterociklil, koji može biti prema potrebi supstituiran, pri čemu je bilo koji izborni supstituent neovisno odabran iz skupine koja se sastoji od C1-10 alkil; C3-6 cikloalkil; hidroksialkil; C1-10 alkoksi; C2-10 alkenil; C2-10 alkinil; C6-C12 aril; ariloksi; heteroaril; heterociklil; halo; hidroksil; halogenirani alkil; amino; alkilamino; arilamino; acil; amido; CN; NO2; N3; CH2OH; CONH2; CONR24R25; CO2R24; CH2OR24; NHCOR24; NHCO2R24; C1-3 alkiltio; sulfat; sulfonska kiselina; sulfonatni esteri; fosfonska kiselina; fosfat; fosfonat; mono-, di- ili trifosfatni esteri; tritil; monometoksitrtil; R24SO; R24SO2; CF3S; CF3SO2; i trialkilsilil; pri čemu su R24 i R25 svaki neovisno odabrani između H i C1-10 alkila.4. A compound according to any of the preceding claims, characterized in that R1 is nitrogen heterocyclyl, which may be optionally substituted, wherein any optional substituent is independently selected from the group consisting of C1-10 alkyl; C3-6 cycloalkyl; hydroxyalkyl; C1-10 Alkoxy; C2-10 alkenyl; C2-10 alkynyl; C6-C12 aryl; aryloxy; heteroaryl; heterocyclyl; halo; hydroxyl; halogenated alkyl; amino; alkylamino; arylamino; acyl; amido; CN; NO2; N3; CH2OH; CONH2; CONR24R25; CO2R24; CH2OR24; NHCOR24; NHCO2R24; C1-3 alkylthio; sulfate; sulfonic acid; sulfonate esters; phosphonic acid; phosphate; phosphonate; mono-, di- or triphosphate esters; trityl; monomethoxytrtyl; R24SO; R24SO2; CF3S; CF3SO2; and trialkylsilyl; wherein R 24 and R 25 are each independently selected from H and C 1-10 alkyl. 5. Spoj prema bilo kojem od prethodnih zahtjeva, naznačen time, da je R1 odabran iz skupine koju čine tetrahidrofuran, tetrahidropiran, piran, pirolidin, morfolin, piperazin i piperidin, koji svi mogu biti prema potrebi supstituirani, pri čemu je bilo koji izborni supstituent neovisno odabran iz skupine koju čine C1-10 alkil; C3-6 cikloalkil; hidroksialkil; C1-10 alkoksi; C2-10 alkenil; C2-10 alkinil; C6-C12 aril; ariloksi; heteroaril; heterociklil; halo; hidroksil; halogenirani alkil; amino; alkilamino; arilamino; acil; amido; CN; NO2; N3; CH2OH; CONH2; CONR24R25; CO2R24; CH2OR24; NHCOR24; NHCO2R24;; C1-3 alkiltio; sulfat; sulfonska kiselina; sulfonatni esteri; fosfonska kiselina; fosfat; fosfonat; mono-, di- ili trifosfatni esteri; tritil; monometoksitrtil; R24SO; R24SO2; CF3S; CF3SO2; i trialkilsilil; pri čemu su R24 i R25 svaki neovisno odabrani između H i C1-10 alkila.5. A compound according to any of the preceding claims, characterized in that R1 is selected from the group consisting of tetrahydrofuran, tetrahydropyran, pyran, pyrrolidine, morpholine, piperazine and piperidine, all of which may be optionally substituted, wherein any optional substituent is independently selected from the group consisting of C1-10 alkyl; C3-6 cycloalkyl; hydroxyalkyl; C1-10 Alkoxy; C2-10 alkenyl; C2-10 alkynyl; C6-C12 aryl; aryloxy; heteroaryl; heterocyclyl; halo; hydroxyl; halogenated alkyl; amino; alkylamino; arylamino; acyl; amido; CN; NO2; N3; CH2OH; CONH2; CONR24R25; CO2R24; CH2OR24; NHCOR24; NHCO2R24;; C1-3 alkylthio; sulfate; sulfonic acid; sulfonate esters; phosphonic acid; phosphate; phosphonate; mono-, di- or triphosphate esters; trityl; monomethoxytrtyl; R24SO; R24SO2; CF3S; CF3SO2; and trialkylsilyl; wherein R 24 and R 25 are each independently selected from H and C 1-10 alkyl. 6. Spoj prema bilo kojem od prethodnih zahtjeva, naznačen time, da je R1 odabran iz skupine koju čine tetrahidrofuran, tetrahidropiran, pirolidin, morfolin, piperazin i piperidin, koji svi mogu biti prema potrebi supstituirani, pri čemu je bilo koji izborni supstituent neovisno odabran iz skupine koju čine C1-10 alkil; C3-6 cikloalkil; hidroksialkil; C1-10 alkoksi; C2-10 alkenil; C2-10 alkinil; C6-C12 aril; ariloksi; heteroaril; heterociklil; halo; hidroksil; halogenirani alkil; amino; alkilamino; arilamino; acil; amido; CN; NO2; N3; CH2OH; CONH2; CONR24R25; CO2R24; CH2OR24; NHCOR24; NHCO2R24; C1-3 alkiltio; sulfat; sulfonska kiselina; sulfonatni esteri; fosfonska kiselina; fosfat; fosfonat; mono-, di- ili trifosfatni esteri; tritil; monometoksitrtil; R24SO; R24SO2; CF3S; CF3SO2; i trialkilsilil; pri čemu su R24 i R25 svaki neovisno odabrani između H i C1-10 alkila.6. A compound according to any of the preceding claims, characterized in that R1 is selected from the group consisting of tetrahydrofuran, tetrahydropyran, pyrrolidine, morpholine, piperazine and piperidine, all of which may be optionally substituted, wherein any optional substituent is independently selected from the group consisting of C1-10 alkyl; C3-6 cycloalkyl; hydroxyalkyl; C1-10 Alkoxy; C2-10 alkenyl; C2-10 alkynyl; C6-C12 aryl; aryloxy; heteroaryl; heterocyclyl; halo; hydroxyl; halogenated alkyl; amino; alkylamino; arylamino; acyl; amido; CN; NO2; N3; CH2OH; CONH2; CONR24R25; CO2R24; CH2OR24; NHCOR24; NHCO2R24; C1-3 alkylthio; sulfate; sulfonic acid; sulfonate esters; phosphonic acid; phosphate; phosphonate; mono-, di- or triphosphate esters; trityl; monomethoxytrtyl; R24SO; R24SO2; CF3S; CF3SO2; and trialkylsilyl; wherein R 24 and R 25 are each independently selected from H and C 1-10 alkyl. 7. Spoj prema bilo kojem od prethodnih zahtjeva, naznačen time, da je R1 odabran iz skupine koju čine pirolidin, piperazin i piperidin, a svi oni mogu biti prema potrebi supstituirani, pri čemu je bilo koji izborni supstituent neovisno odabran iz skupine koju čine C1-10 alkil; C3-6 cikloalkil; hidroksialkil; C1-10 alkoksi; C2-10 alkenil; C2-10 alkinil; C6-C12 aril; ariloksi; heteroaril; heterociklil; halo; hidroksil; halogenirani alkil; amino; alkilamino; arilamino; acil; amido; CN; NO2; N3; CH2OH; CONH2; CONR24R25; CO2R24; CH2OR24; NHCOR24; NHCO2R24; C1-3 alkiltio; sulfat; sulfonska kiselina; sulfonatni esteri; fosfonska kiselina; fosfat; fosfonat; mono-, di- ili trifosfatni esteri; tritil; monometoksitrtil; R24SO; R24SO2; CF3S; CF3SO2; i trialkilsilil; pri čemu su R24 i R25 svaki neovisno odabrani između H i C1-10 alkila.7. A compound according to any of the preceding claims, characterized in that R1 is selected from the group consisting of pyrrolidine, piperazine and piperidine, all of which may be optionally substituted, wherein any optional substituent is independently selected from the group consisting of C1 -10 alkyl; C3-6 cycloalkyl; hydroxyalkyl; C1-10 Alkoxy; C2-10 alkenyl; C2-10 alkynyl; C6-C12 aryl; aryloxy; heteroaryl; heterocyclyl; halo; hydroxyl; halogenated alkyl; amino; alkylamino; arylamino; acyl; amido; CN; NO2; N3; CH2OH; CONH2; CONR24R25; CO2R24; CH2OR24; NHCOR24; NHCO2R24; C1-3 alkylthio; sulfate; sulfonic acid; sulfonate esters; phosphonic acid; phosphate; phosphonate; mono-, di- or triphosphate esters; trityl; monomethoxytrtyl; R24SO; R24SO2; CF3S; CF3SO2; and trialkylsilyl; wherein R 24 and R 25 are each independently selected from H and C 1-10 alkyl. 8. Spoj prema bilo kojem od zahtjeva 1, 2, 3, 5 ili 6, naznačen time, da je R1 odabran iz skupine koja se sastoji od: [image] i u kombinaciji sa svakom takvom R1 skupinom, R2 se neovisno bira iz skupine koju čine: [image] [image] [image] [image] 8. A compound according to any one of claims 1, 2, 3, 5 or 6, characterized in that R1 is selected from the group consisting of: [image] and in combination with each such R1 group, R2 is independently selected from the group consisting of: [image] [image] [image] [image] 9. Spoj prema bilo kojem od prethodnih zahtjeva, naznačen time, da se R2 bira između: [image] pri čemu su Y i R5 definirani u bilo kojem od prethodnih zahtjeva.9. A compound according to any of the preceding claims, characterized in that R2 is selected from: [image] wherein Y and R5 are as defined in any of the preceding claims. 10. Spoj prema bilo kojem od prethodnih zahtjeva, naznačen time, da se R2 bira između: [image] pri čemu je svaka incidencija Y ugljik, a R5 je vodik ili halo.10. A compound according to any of the preceding claims, characterized in that R2 is selected from: [image] wherein each occurrence of Y is carbon and R 5 is hydrogen or halo. 11. Spoj prema bilo kojem od prethodnih zahtjeva, naznačen time, da je R2 odabran između supstituiranog ili hidrogeniranog indacena, 2,6-dialkilfenila, 2,6-dialkil-4-halofenila, 2,6-dicikloalkilfenila i 2,6-dicikloalkil-4-halofenila.11. A compound according to any of the preceding claims, characterized in that R2 is selected from substituted or hydrogenated indacene, 2,6-dialkylphenyl, 2,6-dialkyl-4-halophenyl, 2,6-dicycloalkylphenyl and 2,6-dicycloalkyl -4-halophenyl. 12. Spoj prema bilo kojem od prethodnih zahtjeva, naznačen time, da je R2 odabran između heksahidroindacena, 2,6-diizopropilfenil, 2,6-diizopropil-4-klorofenil, 2,6-diciklopropilfenil i 2,6-diciklopropil-4-klorofenila.12. A compound according to any of the preceding claims, characterized in that R2 is selected from hexahydroindacene, 2,6-diisopropylphenyl, 2,6-diisopropyl-4-chlorophenyl, 2,6-dicyclopropylphenyl and 2,6-dicyclopropyl-4- chlorophenyl. 13. Spoj prema bilo kojem od prethodnih zahtjeva, naznačen time, da je J atom sumpora.13. A compound according to any of the preceding claims, characterized in that J is a sulfur atom. 14. Spoj prema bilo kojem od prethodnih zahtjeva, naznačen time, da je W atom kisika.14. A compound according to any of the preceding claims, characterized in that W is an oxygen atom. 15. Spoj prema bilo kojem od prethodnih zahtjeva, naznačen time, da je spoj spoj formule (Ia), (Ib) ili (Ic), ili njegova farmaceutski prihvatljiva sol ili solvat: [image] pri čemu je R1 definiran u bilo kojem od prethodnih zahtjeva.15. A compound according to any of the preceding claims, characterized in that the compound is a compound of formula (Ia), (Ib) or (Ic), or a pharmaceutically acceptable salt or solvate thereof: [image] wherein R 1 is as defined in any of the preceding claims. 16. Spoj prema bilo kojem od zahtjeva 1-3, 5-6 ili 8-15, naznačen time, da je spoj odabran iz skupine koju čine: [image] i njihove farmaceutski prihvatljive soli i solvati.16. A compound according to any one of claims 1-3, 5-6 or 8-15, characterized in that the compound is selected from the group consisting of: [image] and pharmaceutically acceptable salts and solvates thereof. 17. Farmaceutski pripravak, naznačen time što sadrži spoj prema bilo kojem od zahtjeva 1 do 16, ili njegova farmaceutski prihvatljiva sol ili solvat, i farmaceutski prihvatljiv nosač, razrjeđivač i/ili pomoćnu tvar.17. Pharmaceutical preparation, characterized in that it contains a compound according to any one of claims 1 to 16, or a pharmaceutically acceptable salt or solvate thereof, and a pharmaceutically acceptable carrier, diluent and/or auxiliary substance. 18. Spoj ili farmaceutski prihvatljiva sol ili solvat prema bilo kojem od zahtjeva 1 do 16, naznačen time, da se koristi u medicini.18. A compound or a pharmaceutically acceptable salt or solvate according to any one of claims 1 to 16, characterized in that it is used in medicine. 19. Spoj ili farmaceutski prihvatljiva sol ili solvat prema bilo kojem od zahtjeva 1 do 16, naznačen time, da se koristi u liječenju ili prevenciji navedenih: (a) bolest, poremećaj ili stanje imunološkog sustava; i/ili (b) upalna bolest, poremećaj ili stanje ili autoimuna bolest, poremećaj ili stanje; i/ili (c) bolest, poremećaj ili stanje kože; i/ili (d) bolest, poremećaj ili stanje kardiovaskularnog sustava; i/ili (e) rak, tumor ili drugi zloćudni tumor; i/ili (f) bolest, poremećaj ili stanje bubrežnog sustava; i/ili (g) bolest, poremećaj ili stanje gastrointestinalnog trakta; i/ili (h) bolest, poremećaj ili stanje dišnog sustava; i/ili (i) bolest, poremećaj ili stanje endokrinog sustava; i/ili (j) bolest, poremećaj ili stanje središnjeg živčanog sustava (CNS); i/ili (k) bolest, poremećaj ili stanje odabrano iz skupine koja se sastoji od konstitutivne upale, uključujući periodične sindrome povezane s kriopirinom (CAPS): Muckle-Wellsov sindrom (MWS), obiteljski hladni autoinflamatorni sindrom (FCAS) i multisustavna upalna bolest s novorođenčetom (NOMID); uključujući autoinflamatorne bolesti: obiteljska mediteranska groznica (FMF), periodični sindrom povezan s TNF receptorima (TRAPS), nedostatak mevalonate kinaze (MKD), hiperimunoglobulinemija D i sindrom periodične groznice (HIDS), nedostatak antagonista receptora za interleukin 1 (DIRA), Majeedov sindrom, piogeni artritis, gangrenozna piodermija i akne (PAPA), haploinsuficijencija A20 (HA20), dječji granulomatozni artritis (PGA), nedostatak protutijela povezan s PLCG2 i imunološka disregulacija (PLAID), autoinflamacija povezana s PLCG2, nedostatak protutijela i imunološka disregulacija , sideroblastična anemija s imunodeficijencijom B-stanica, periodična groznica i zastoj u razvoju (SIFD); Sweetov sindrom, kronični nebakterijski osteomijelitis (CNO), kronični recidivni multifokalni osteomijelitis (CRMO) i sinovitis, akne, pustuloza, hiperostoza, sindrom osteitisa (SAPHO); autoimune bolesti, uključujući multiple sklerozu (MS), dijabetes tipa 1, psorijazu, reumatoidni artritis, Behcetovu bolest, Sjogrenov sindrom i Schnitzlerov sindrom; respiratorne bolesti, uključujući kronični opstruktivni plućni poremećaj (KOPB), steroidno rezistentna astma, azbestoza, silikoza i cistična fibroza; bolesti središnjeg živčanog sustava, uključujući Parkinsonovu bolest, Alzheimerovu bolest, bolest motornih neurona, Huntingtonovu bolest, cerebralnu malariju i ozljedu mozga od pneumokoknog meningitisa; metaboličke bolesti, uključujući dijabetes tipa 2, aterosklerozu, pretilost, giht, pseudo-giht; očne bolesti, uključujući one očnog epitela, starosnu degeneraciju makule (AMD), infekciju rožnice, uveitis i suho oko; bolesti bubrega, uključujući kroničnu bolest bubrega, oksalatnu nefropatiju i dijabetičku nefropatiju; bolesti jetre, uključujući bezalkoholni steatohepatitis i alkoholnu bolest jetre; upalne reakcije na koži, uključujući kontaktnu preosjetljivost i opekline; upalne reakcije u zglobovima, uključujući osteoartritis, sistemski juvenilni idiopatski artritis, Stillova bolest kod odraslih, recidivirajući polihondritis; virusne infekcije, uključujući alfa virus, uključujući Chikungunya i rijeku Ross, i flavivirus, uključujući denga i zika viruse, gripu, HIV; hidradenitis suppurativa (HS) i druge kožne bolesti koje uzrokuju ciste; karcinomi, uključujući metastaze raka pluća, karcinom gušterače, rak želuca, mijelodisplastični sindrom, leukemija; polimiozitis; moždani udar; infarkt miokarda; Kalemljenje naspram bolesti domaćina; hipertenzija; kolitis; infekcija helminthima; bakterijska infekcija; aneurizam trbušne aorte; zarastanje rana; depresija, psihološki stres; perikarditis, uključujući Dresslerov sindrom, reperfuzijsku ozljedu ishemije i bilo koju bolest kod koje je utvrđeno da pojedinac nosi zametnu liniju ili somatsku netihu mutaciju u NLRP3.19. A compound or a pharmaceutically acceptable salt or solvate according to any one of claims 1 to 16, characterized in that it is used in the treatment or prevention of the following: (a) disease, disorder or condition of the immune system; and/or (b) an inflammatory disease, disorder or condition or an autoimmune disease, disorder or condition; and/or (c) a disease, disorder or condition of the skin; and/or (d) disease, disorder or condition of the cardiovascular system; and/or (e) cancer, tumor or other malignant tumor; and/or (f) disease, disorder or condition of the renal system; and/or (g) disease, disorder or condition of the gastrointestinal tract; and/or (h) disease, disorder or condition of the respiratory system; and/or (i) disease, disorder or condition of the endocrine system; and/or (j) central nervous system (CNS) disease, disorder or condition; and/or (k) a disease, disorder or condition selected from the group consisting of constitutive inflammation, including cryopyrin-associated periodic syndromes (CAPS): Muckle-Wells syndrome (MWS), familial cold autoinflammatory syndrome (FCAS), and multisystem inflammatory disease of the newborn ( NOMID); including autoinflammatory diseases: familial Mediterranean fever (FMF), TNF receptor-associated periodic syndrome (TRAPS), mevalonate kinase deficiency (MKD), hyperimmunoglobulinemia D and periodic fever syndrome (HIDS), interleukin 1 receptor antagonist (DIRA) deficiency, Majeed syndrome , pyogenic arthritis, pyoderma gangrenosum and acne (PAPA), haploinsufficiency A20 (HA20), pediatric granulomatous arthritis (PGA), PLCG2-associated antibody deficiency and immune dysregulation (PLAID), PLCG2-associated autoinflammation, antibody deficiency and immune dysregulation , sideroblastic anemia with B-cell immunodeficiency, periodic fever and developmental delay (SIFD); Sweet's syndrome, chronic nonbacterial osteomyelitis (CNO), chronic recurrent multifocal osteomyelitis (CRMO) and synovitis, acne, pustulosis, hyperostosis, osteitis syndrome (SAPHO); autoimmune diseases, including multiple sclerosis (MS), type 1 diabetes, psoriasis, rheumatoid arthritis, Behcet's disease, Sjogren's syndrome and Schnitzler's syndrome; respiratory diseases, including chronic obstructive pulmonary disorder (COPD), steroid-resistant asthma, asbestosis, silicosis and cystic fibrosis; diseases of the central nervous system, including Parkinson's disease, Alzheimer's disease, motor neuron disease, Huntington's disease, cerebral malaria and brain injury from pneumococcal meningitis; metabolic diseases, including type 2 diabetes, atherosclerosis, obesity, gout, pseudo-gout; eye diseases, including those of the eye epithelium, age-related macular degeneration (AMD), corneal infection, uveitis, and dry eye; kidney diseases, including chronic kidney disease, oxalate nephropathy and diabetic nephropathy; liver diseases, including non-alcoholic steatohepatitis and alcoholic liver disease; inflammatory skin reactions, including contact hypersensitivity and burns; inflammatory reactions in the joints, including osteoarthritis, systemic juvenile idiopathic arthritis, Still's disease in adults, relapsing polychondritis; viral infections, including alpha virus, including Chikungunya and Ross River, and flavivirus, including dengue and zika viruses, influenza, HIV; hidradenitis suppurativa (HS) and other skin diseases that cause cysts; cancers, including lung cancer metastases, pancreatic cancer, stomach cancer, myelodysplastic syndrome, leukemia; polymyositis; stroke; myocardial infarction; Grafting against host disease; hypertension; colitis; helminth infection; bacterial infection; abdominal aortic aneurysm; wound healing; depression, psychological stress; pericarditis, including Dressler syndrome, ischemia reperfusion injury, and any disease in which an individual is found to carry a germline or somatic non-silent mutation in NLRP3. 20. Spoj ili farmaceutski prihvatljiva sol ili solvat prema bilo kojem od zahtjeva 1 do 16, naznačen time, da se koristi za dijagnosticiranje bolesti, poremećaja ili stanja kod sisavaca, uključujući korak davanja obilježenog spoja prema bilo kojem od zahtjeva 1 do 16., ili njihova farmaceutski prihvatljiva sol ili solvat, ili njegov kompleks helata metalnih iona, sisavcu ili biološkom uzorku dobivenom od sisavca radi olakšavanja dijagnoze bolesti, poremećaja ili stanja sisavca.20. A compound or a pharmaceutically acceptable salt or solvate according to any one of claims 1 to 16, characterized in that it is used to diagnose a disease, disorder or condition in a mammal, including the step of administering a labeled compound according to any one of claims 1 to 16, or a pharmaceutically acceptable salt or solvate thereof, or a metal ion chelate complex thereof, to a mammal or a biological sample obtained from the mammal to facilitate the diagnosis of a disease, disorder or condition of the mammal.
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